Journal
FRONTIERS IN PHYSIOLOGY
Volume 13, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fphys.2022.809845
Keywords
spinal cord injury; visceral adipose tissue; mitochondria; inflammation; growth factors; testosterone
Categories
Funding
- DoD-CDMRP [W81XWH-14-SCIRP-CTA]
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This study investigated the predictors of mitochondrial health in individuals with chronic spinal cord injury (SCI), focusing on visceral adiposity, inflammatory biomarkers, testosterone, and circulating serum growth factors. The results showed that increased visceral adiposity and associated inflammatory signaling, along with reduced testosterone levels, predicted mitochondrial dysfunction following SCI. Specifically, lower visceral adiposity and higher testosterone levels or lower visceral adiposity and lower inflammation levels positively predicted mitochondrial mass and enzyme activity in individuals with chronic SCI.
Background: Mitochondrial health is an important predictor of several health-related comorbidities including obesity, type 2 diabetes mellitus, and cardiovascular disease. In persons with spinal cord injury (SCI), mitochondrial health has been linked to several important body composition and metabolic parameters. However, the complex interplay of how mitochondrial health is affected has yet to be determined in this population. Objective: In this study, we examined the contribution of visceral adiposity, inflammatory biomarkers, testosterone and circulating serum growth factors as predictors of mitochondrial health in persons with chronic SCI. ParticipantsThirty-three individuals with chronic SCI (n = 27 Males, n = 6 Females, age: 40 +/- 13.26 years, level of injury: C4-L1, BMI: 23 +/- 5.57) participated in this cross-sectional study. Methods: Visceral adipose tissue (VAT) was measured via magnetic resonance imaging (MRI). After an overnight fast, serum testosterone, inflammatory biomarkers [interleukin 6 (IL-6), tumor necrosis factor alpha (TNF-alpha), c-reactive protein (CRP)], and anabolic growth factors [insulin-like growth factor 1 (IGF-1), insulin-like growth factor binding protein 3 (IGFBP-3)] were measured. Skeletal muscle biopsies were obtained from the vastus lateralis muscle to measure citrate synthase (CS) and Complex III activity. Regression analyses were used to examine predictors of mitochondrial mass and activity. Results: CS activity was negatively associated with VAT (r(2) = 0.360, p < 0.001), CRP (r(2) = 0.168, p = 0.047), and positively associated with testosterone (r(2) = 0.145, p = 0.042). Complex III activity was negatively associated with VAT relative to total lean mass (VAT:TLM) (r(2) = 0.169, p = 0.033), trended for CRP (r(2) = 0.142, p = 0.069), and positively associated with testosterone (r(2) = 0.224, p = 0.010). Multiple regression showed CS activity was significantly associated with VAT + CRP (r(2) = 0.412, p = 0.008) and VAT + Testosterone (r(2) = 0.433, p = 0.001). Complex III activity was significantly associated with VAT relative to total trunk cross-sectional area (CSA) + CRP (VAT:total trunk CSA + CRP; r(2) = 0.286, p = 0.048) and VAT + Testosterone (r(2) = 0.277, p = 0.024). Conclusion: Increased visceral adiposity and associated inflammatory signaling (CRP) along with reduced testosterone levels predict mitochondrial dysfunction following SCI. Specifically, lower VAT(CSA) and higher testosterone levels or lower VAT(CSA) and lower CRP levels positively predict mitochondrial mass and enzyme activity in persons with chronic SCI. Future research should investigate the efficacy of diet, exercise, and potentially testosterone replacement therapy on enhancing mitochondrial health in chronic SCI.
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